EP1572260A2 - Thin-walled polyurethane articles - Google Patents
Thin-walled polyurethane articlesInfo
- Publication number
- EP1572260A2 EP1572260A2 EP03757309A EP03757309A EP1572260A2 EP 1572260 A2 EP1572260 A2 EP 1572260A2 EP 03757309 A EP03757309 A EP 03757309A EP 03757309 A EP03757309 A EP 03757309A EP 1572260 A2 EP1572260 A2 EP 1572260A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- thin
- molecular sieve
- article
- poiyurethane
- walled
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000004814 polyurethane Substances 0.000 title description 15
- 229920002635 polyurethane Polymers 0.000 title description 9
- 239000002808 molecular sieve Substances 0.000 claims abstract description 36
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims abstract description 36
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 41
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000010410 layer Substances 0.000 claims description 13
- 230000005540 biological transmission Effects 0.000 claims description 11
- 229920001971 elastomer Polymers 0.000 claims description 9
- 239000000806 elastomer Substances 0.000 claims description 9
- 239000002344 surface layer Substances 0.000 claims description 8
- 239000004970 Chain extender Substances 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 6
- 125000005442 diisocyanate group Chemical group 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 125000004427 diamine group Chemical group 0.000 claims 1
- 229920003225 polyurethane elastomer Polymers 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 22
- 238000007598 dipping method Methods 0.000 description 12
- 238000012360 testing method Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- 150000002334 glycols Chemical class 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 6
- -1 poly(ethyleneether) Polymers 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 5
- 229920006267 polyester film Polymers 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000004927 clay Substances 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- ZWVMLYRJXORSEP-LURJTMIESA-N (2s)-hexane-1,2,6-triol Chemical compound OCCCC[C@H](O)CO ZWVMLYRJXORSEP-LURJTMIESA-N 0.000 description 1
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- FGNLEIGUMSBZQP-UHFFFAOYSA-N cadaverine dihydrochloride Chemical compound Cl.Cl.NCCCCCN FGNLEIGUMSBZQP-UHFFFAOYSA-N 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000001010 compromised effect Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000002182 crystalline inorganic material Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- GEQHKFFSPGPGLN-UHFFFAOYSA-N cyclohexane-1,3-diamine Chemical compound NC1CCCC(N)C1 GEQHKFFSPGPGLN-UHFFFAOYSA-N 0.000 description 1
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000013618 particulate matter Substances 0.000 description 1
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 0.000 description 1
- 229920005548 perfluoropolymer Polymers 0.000 description 1
- 229920000163 poly(trimethylene ether) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000934 spermatocidal agent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 230000003655 tactile properties Effects 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004636 vulcanized rubber Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
- C08L75/12—Polyurethanes from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B42/00—Surgical gloves; Finger-stalls specially adapted for surgery; Devices for handling or treatment thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F6/00—Contraceptive devices; Pessaries; Applicators therefor
- A61F6/02—Contraceptive devices; Pessaries; Applicators therefor for use by males
- A61F6/04—Condoms, sheaths or the like, e.g. combined with devices protecting against contagion
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/04—Macromolecular materials
- A61L31/06—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/346—Clay
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L3/00—Compositions of starch, amylose or amylopectin or of their derivatives or degradation products
- C08L3/02—Starch; Degradation products thereof, e.g. dextrin
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/1376—Foam or porous material containing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/251—Mica
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/252—Glass or ceramic [i.e., fired or glazed clay, cement, etc.] [porcelain, quartz, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/256—Heavy metal or aluminum or compound thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/259—Silicic material
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31554—Next to second layer of polyamidoester
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31786—Of polyester [e.g., alkyd, etc.]
Definitions
- This invention relates to low-tack thin-walled articles comprising a poiyurethane elastomer, for example surgical gloves, clean-room gloves, condoms, and the like. More particularly, the invention relates to such elastomeric articles containing specific amounts of molecular sieve.
- Elastomeric gloves are known for use in sterile, surgical, and chemical environments.
- United States Patents US2814834 Hess et al.
- US3553308 Kelashi et al.
- US5132129 Patent et al.
- United States Patents US5391343 Disibelbis et al.
- US5728340 Disibelbis et al. described processes for making poiyurethane thin-walled articles, such as gloves and condoms, which have superior mechanical properties, for example low set and high resistance to tear and puncture.
- a problem characteristic of elastomeric thin-walled articles like gloves is surface tack, which can result in difficulty removing a glove from the mandrel during manufacture or from its package, and/or difficulty in donning a glove.
- United States Patent US6016570 discloses the use of powder and lubricant additives and of contact- reducing textures formed by intermittent spray coating (optionally containing fillers to reduce droplet size) to control tack of vinyl gloves.
- lubricants can contaminate clean rooms and operating rooms, and surface textures can reduce tactility.
- the present invention provides a thin-walled article comprising at least one surface layer of: a poiyurethane elastomer; and about 20 to 40 weight percent, based on the weight of the layer, of a molecular sieve having a mean particle size of about 1 to 15 microns and less than 1 weight percent, based on weight of molecular sieve, of particle size greater than about 40 microns.
- thin-walled articles containing certain amounts of molecular sieve have an unexpected combination of very low tack, low porosity, reduced set and stress, smooth hand, no particulate visible to the unaided eye, and only slightly opaque appearance.
- the low tack is advantageous for removing the article from a package and for donning, the low porosity for good barrier protection in clean room and medical environments, the reduced set and stress for better shape retention and improved comfort, and the tactile and visual properties for good aesthetics.
- thin-walled refers to a thickness of no greater than about 0.18 millimeters.
- the article can be said to have an inner surface and an outer surface, preferably identified in the configuration in which the article is to be used.
- Polyurethane refers to a long-chain synthetic polymer comprising alternating "soft segments” comprising primarily polyester, polyether, or polycarbonate and “hard segments” derived from the reaction of a diisocyanate and a difunctional chain extender.
- “Elastomer” means a polymer which, free of diluents, retracts to less than 1.5 times its original length within one minute after being stretched at room temperature to twice its original length and held for one minute before release.
- Molecular sieve means a crystalline inorganic material having pores, cavities, or other interstices which are uniformly on the order of Angstroms in size and includes synthetic and natural zeolites, which can be alumino-silicates, titano-silicates, and the like.
- the thin-walled article of the invention comprises at least one surface layer of a poiyurethane elastomer and about 20 to 40 wt% (preferably about 25 to 35 wt%), based on the weight of the layer , of a molecular sieve having a mean particle size of about 1 to 15 microns and less than about 1 wt%, based on weight of molecular sieve, of particle size greater than about 40 microns.
- the article can have a stress at 100% extension of no greater than about 200 psi (1.4 megaPascals), a "calculated water vapor transmission rate" of less than about 50 g/hr/m 2 (preferably less than about 20 g/hr/m 2 ), calculated for an 0.1 mm thick sample, and a percent set of less than about 25%.
- Elastomeric polyurethanes useful in this invention can be prepared by reacting a polymeric glycol with a diisocyanate to form an isocyanate- terminated prepolymer (a "capped glycol”), preferably having an isocyanate (NCO) end-group concentration in the range of about 1.4 to 2.0%.
- the capped glycol can be dissolved in a suitable solvent, and then reacting the capped glycol with a difunctional chain extender having active hydrogen atoms.
- suitable solvents for preparing solutions of such polymers are amide solvents such as dimethylacetamide (“DMAc”), dimethylformamide, and N-methylpyrrolidone, but other solvents such as dimethylsulfoxide and tetramethylurea can also be used.
- Polymeric glycols used in the preparation of the elastomeric polyurethanes include polyether glycols, polyester glycols, polycarbonate glycols and copolymers thereof.
- glycols examples include poly(ethyleneether) glycol, poly(trimethyleneether) glycol, poly(tetramethyleneether) glycol, poly(tetramethylene-co-2- methyltetramethyleneether) glycol, poly(ethyiene-co-butylene adipate) glycol, poly(2,2-dimethyl-1 ,3-propylene dodecanedioate) glycol, poly(3- methyl-1 ,5-pentamethylene dodecanedioate) glycol, poly(pentane-1 ,5- carbonate) glycol, and poly(hexane-1 ,6-carbonate) glycol.
- Polyester glycols having a number average molecular weight of about 3,000 to 6,000 are preferred.
- Polyester glycols derived from the reaction of adipic acid with a mixture of ethylene glycol and 1 ,4-butanediol (mole ratio of 30:70 to 75:25) are more preferred.
- Useful diisocyanates include 1-isocyanato-4-[(4'- isocyanatophenyl)methyl]benzene (preferred), 1 -isocyanato-2-[(4'- isocyanato-phenyl)methyl]benzene, isophorone diisocyanate, 1 ,6- hexanediisocyanate, 2,4-tolylene diisocyanate, and mixtures thereof.
- the chain extender can be a diol, an aminoalcohol, or a diamine.
- Useful diols include ethylene glycol, 1 ,3-trimethylene glycol, 1 ,4- butanediol, and mixtures thereof.
- the chain extender is a diol
- the poiyurethane can be prepared using the two-step prepolymer method described hereinabove or using a one-step method in which the ingredients are mixed together at substantially the same time.
- Useful diamines include ethylene diamine (preferred), 1 ,2-propanediamine, 2- methyl-1 ,5-pentanediamine, 1 ,3-diaminopentane, 1 ,4-cyclohexane- diamine, 1 ,3-cyclohexanediamine, and mixtures thereof.
- the two-step, prepolymer polymerization method is generally used.
- Monofunctional amine chain terminators such as diethyl amine, butylamine, cyclohexylamine, and the like can be added to control the molecular weight of the polymer, and small amounts of trifunctional ingredients such as diethylenetriamine can be added for solution viscosity control.
- the solution of poiyurethane can have a falling ball viscosity of about 25 to 125 poise and a poiyurethane concentration of about 12 to 20 wt%, based on the total weight of the solution.
- the molecular sieve can be mixed directly into the poiyurethane solution, or optionally prepared first as a concentrated slurry or masterbatch which can then be added to the main poiyurethane solution.
- the molecular sieve can generally be used as-received from the supplier; however if it has been exposed to water or water vapor, it can be advantageous to dry it before use to reduce the risk of increased gel formation in the dipping mixture, but such a problem was not observed in the present work.
- the addition of the molecular sieve can result in increased viscosity of the mixture compared to the poiyurethane solution, but this can be easily reduced to about that of the poiyurethane solution by adding more solvent.
- the thin-walled article can be prepared as follows.
- the dipping mixture of poiyurethane and molecular sieve which can be prepared as described hereinabove and maintained at about 20°C to 30°C, can be degassed by subjecting it to vacuum for a few minutes to remove entrapped and/or dissolved air.
- a ceramic or aluminum mandrel of the desired size and shape, optionally heated and having a matte finish, can then be dipped into the degassed solution, preferably at an angle of about 80° to almost 90° with, in the case of a glove mandrel, the fingers entering the mixture first and the palm facing upward.
- the mandrel can be kept in the mixture for about 5 to 30 seconds, removed over a period of 10 to 15 seconds, and allowed to drain for about 1 to 5 minutes.
- the coated mandrel can then be inverted, dried for a sufficient time and at a sufficient temperature to remove the solvent, and allowed to cool.
- the glove can then be stripped from the mandrel by eversion. Dipping the coated mandrel into water optionally containing surfactants can assist in stripping the article from the mandrel.
- the thin-walled article comprises at least one surface layer of poiyurethane elastomer containing molecular sieve.
- Other layers can be applied by carrying out other dipping steps, either before or after applying the layer containing molecular sieve.
- at least one layer containing molecular sieve is a surface layer of the article.
- thin layers for example comprising microbic.de, spermicide, and the like, can be applied over a molecular-sieve containing surface layer, provided the benefits of the invention are not compromised.
- the mandrel can be pre-heated, for example to about 85°C, before the first dip to help avoid nonuniformities in the thin-walled article.
- a first dipping step can be into a poiyurethane solution substantially free of molecular sieve
- a second dipping step can be into the polyurethane/molecular sieve mixture, so that only one layer of the article contains the molecular sieve.
- the thin-walled article can then have a molecular sieve-containing poiyurethane elastomer inner surface layer for easy donning and a poiyurethane elastomer outer, second, layer substantially free of molecular sieve but having a matte finish for easy removal from a package.
- such later dipping step(s) can also be made to limited, appropriate depths so that the polyurethane/molecular sieve mixture is applied only to pre-selected portions of the coated mandrel, for example to add thickness and reduce tack only in the finger or finger-and- palm portions of a glove.
- release agents such as perfluoropolymers or silicone oil can optionally be applied to the mandrel before dipping it into the mixture or added directly to the dipping mixture, such agents have not typically been found necessary in the inventive process. This is an advantage for clean room and medical use, because release agents are potentially extractable.
- the particulate additives were used as received from the supplier.
- the poiyurethane solution viscosity was determined in accordance with the general method of ASTM D1343-69 with a Model DV- 8 Falling Ball Viscometer, (sold by Duratech Corp., Waynesboro, VA), operated at 40°C.
- Water vapor transmission rates used as a guide to porosity and barrier properties, were determined according to the method of ASTM E96-94, "Standard Test Method for Water Vapor Transmission of Materials, Water Method".
- ASTM E96-94 Standard Test Method for Water Vapor Transmission of Materials, Water Method.
- a 1.5 mil (0.038 mm) thick film sample was clamped without stretching to a flanged aluminum test cup having a mouth area of 31.7 cm 2 and containing 1.5 cm of distilled water whose surface was 19 mm below the sample.
- the test assembly was weighed and then placed in a test chamber held at 24°C and 55% relative humidity and provided with an air flow of 2.8 m/s directed across the surface of the sample. After 24 hours, the test assembly was again weighed, and the loss of water and the water vapor transmission rate were calculated.
- the test was performed on six samples, and the average was recorded. For convenience, calculated water vapor transmission rates are also reported herein as reduced to those of an article having a thickness of 0.1mm
- L b and L a are respectively the film length, when held without tension, before and after the five elongation/relaxation cycles.
- a polyurethaneurea was prepared by reacting a 3400 number- average molecular weight polyester glycol (the reaction product of a 60/40 mole ratio mixture of ethylene glycol and 1 ,4-butanediol with adipic acid) with 1-isocyanato-4-[(4-isocyanatophenyl)methyl]benzene (1.80 %NCO, mole ratio of diisocyanate to polymeric glycol 1.83:1 ) to form an isocyanate-terminated prepolymer.
- a 3400 number- average molecular weight polyester glycol the reaction product of a 60/40 mole ratio mixture of ethylene glycol and 1 ,4-butanediol with adipic acid
- 1-isocyanato-4-[(4-isocyanatophenyl)methyl]benzene (1.80 %NCO, mole ratio of diisocyanate to polymeric glycol 1.83:1
- the prepolymer was dissolved in DMAc and then chain-extended and -terminated with a mixture of ethylene diamine and cyclohexylamine to form a 17 wt% poiyurethane solution in DMAc.
- the solution viscosity was 115 poise.
- Titanium dioxide Ti-Pure® R-706, a registered trademark of E. I. du Pont de Nemours and Company
- a molecular sieve having an 8 micron mean particle size and less than 1 wt% of a particle size above 18 microns
- Example 1 1.5mil (0.038mm) thick was cast from the polyurethane/molecular sieve mixture with a doctor knife onto polyester film, dried at 80°C-100°C for 20-60 minutes, carefully peeled from the polyester film, and evaluated visually and by hand.
- Comparison Sample 1 Similar films were cast from mixtures of the same poiyurethane and titanium dioxide with no other added particulate (Comparison Sample 1 ), with added kaolin clay powder (VWR Company, 5 micron mean particle size, 0.8 to 26 micron size range) (Comparison Sample 2), with added silica gel (EM Science, 48 micron mean particle size, 7 to 160 micron size range, 90% between 40 and 63 microns) (Comparison Sample 3), with added Zonyl® Fluoroadditive MP1000 low molecular weight polytetrafluoroethylene powder (a registered trademark of E. I.
- Sample 1 and Comparison Sample 1 were evaluated for barrier properties by applying ASTM E96-94.
- Sample 1 containing 30 wt% molecular sieve based on total film weight, was found to have a water vapor transmission rate of 638 g/m 2 over a 24 hour period (calculated to be 10 g/hr/m 2 for an 0.1 mm thick film). That represented only a modest increase over the rate of 514 g/m 2 over a 24 hour period (calculated to be 8 g/hr/m 2 for an 0.1 mm thick film) for Comparison Sample 1 , containing no molecular sieve. Such a low water vapor transmission rate is indicative of good barrier properties.
- Sample 2 was cast onto a polyester film from the same polyurethane/molecular sieve composition as was used for Sample 1 and dried. The resulting 2.8 mil (0.07 mm) thick poiyurethane film, still on the polyester film, was cut to an appropriate size, the poiyurethane film was carefully peeled from the polyester film, and the polyurethane's properties were determined with an Instron® tensile tester.
- Comparison Sample 6 was cast from the same poiyurethane solution composition as Comparison Sample 1 and similarly prepared for testing.
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Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US165660 | 2002-06-07 | ||
US10/165,660 US6720049B2 (en) | 2002-06-07 | 2002-06-07 | Thin-walled polyurethane articles |
PCT/US2003/017258 WO2003103741A2 (en) | 2002-06-07 | 2003-06-03 | Thin-walled polyurethane articles |
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EP1572260A2 true EP1572260A2 (en) | 2005-09-14 |
EP1572260A3 EP1572260A3 (en) | 2005-10-26 |
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EP03757309A Withdrawn EP1572260A3 (en) | 2002-06-07 | 2003-06-03 | Thin-walled polyurethane articles |
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US (1) | US6720049B2 (en) |
EP (1) | EP1572260A3 (en) |
JP (1) | JP4213118B2 (en) |
CN (1) | CN1307225C (en) |
HK (1) | HK1086848A1 (en) |
WO (1) | WO2003103741A2 (en) |
Families Citing this family (11)
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US6772443B2 (en) * | 2002-12-30 | 2004-08-10 | Kimberly-Clark Worldwide, Inc. | Breathable elastomeric glove |
CN101484496B (en) * | 2006-07-12 | 2012-06-27 | 三菱化学株式会社 | Process for producing polyurethane and use of polyurethane obtained by the process |
ZA200709380B (en) * | 2006-11-24 | 2008-11-26 | Csir | Production of membranes |
EP2190642A1 (en) * | 2007-08-30 | 2010-06-02 | Invista Technologies S.A R.L. | Preparation of thin-walled articles of polyurethaneurea |
WO2011004335A2 (en) | 2009-07-09 | 2011-01-13 | Duocure, Inc. | Duodenal liner device and methods and devices for restricting the passage of chyme from the stomach |
US20110198777A1 (en) * | 2010-02-17 | 2011-08-18 | Der-Lin Liou | Method for manufacturing seamless thin-walled articles with thermoplastic materials |
US9707715B2 (en) | 2011-10-31 | 2017-07-18 | Kimberly-Clark Worldwide, Inc. | Elastomeric articles having a welded seam made from a multi-layer film |
US8566965B2 (en) | 2011-10-31 | 2013-10-29 | Kimberly-Clark Worldwide, Inc. | Elastomeric articles having a welded seam that possess strength and elasticity |
JP5966765B2 (en) * | 2012-08-22 | 2016-08-10 | 富士通株式会社 | Information processing system, relay device, information processing program, and information processing method |
CN111658288A (en) * | 2020-05-20 | 2020-09-15 | 兰州科天健康科技股份有限公司 | Pure polyurethane condom with adhesive layer and preparation method thereof |
CN111393694A (en) * | 2020-05-14 | 2020-07-10 | 上海鑫亘环保科技有限公司 | TPU film with good surface polarity and preparation process thereof |
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2002
- 2002-06-07 US US10/165,660 patent/US6720049B2/en not_active Expired - Lifetime
-
2003
- 2003-06-03 CN CNB038131390A patent/CN1307225C/en not_active Expired - Fee Related
- 2003-06-03 EP EP03757309A patent/EP1572260A3/en not_active Withdrawn
- 2003-06-03 JP JP2004510859A patent/JP4213118B2/en not_active Expired - Fee Related
- 2003-06-03 WO PCT/US2003/017258 patent/WO2003103741A2/en not_active Application Discontinuation
-
2006
- 2006-06-20 HK HK06107007A patent/HK1086848A1/en not_active IP Right Cessation
Non-Patent Citations (1)
Title |
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See references of WO03103741A3 * |
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CN1714111A (en) | 2005-12-28 |
CN1307225C (en) | 2007-03-28 |
US6720049B2 (en) | 2004-04-13 |
WO2003103741A2 (en) | 2003-12-18 |
HK1086848A1 (en) | 2006-09-29 |
EP1572260A3 (en) | 2005-10-26 |
JP4213118B2 (en) | 2009-01-21 |
JP2006504811A (en) | 2006-02-09 |
WO2003103741A3 (en) | 2005-09-01 |
US20030228477A1 (en) | 2003-12-11 |
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